Canonical Allele Identifier: CA658166152

Gene: NF2

Linked Data

• COSMIC: COSN22630070

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29695280dup , CM000684.2:g.29695280dup	GRCh38
NC_000022.10:g.30091269dup , CM000684.1:g.30091269dup	GRCh37
NC_000022.9:g.28421269dup	NCBI36
NG_009057.1:g.96725dup , LRG_511:g.96725dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338641.10:c.*478dup MANE Select	ENSP00000344666.5:n.*478dup
ENST00000672461.1:c.*501+37dup	ENSP00000500919.1:n.*501+37dup
ENST00000672896.1:c.*538dup	ENSP00000500117.1:n.*538dup
ENST00000338641.8:c.*478dup	ENSP00000344666.4:n.*478dup
ENST00000361452.8:c.*538dup	ENSP00000354897.4:n.*538dup
ENST00000413209.6:c.*478dup	ENSP00000409921.2:n.*478dup
NM_000268.3:c.*478dup , LRG_511t1:c.*478dup	NP_000259.1:n.*478dup
NM_016418.5:c.*538dup , LRG_511t2:c.*538dup	NP_057502.2:n.*538dup
NM_181828.2:c.*538dup	NP_861966.1:n.*538dup
NM_181829.2:c.*538dup	NP_861967.1:n.*538dup
NM_181830.2:c.*538dup	NP_861968.1:n.*538dup
NM_181832.2:c.*553dup	NP_861970.1:n.*553dup
NM_181833.2:c.*478dup	NP_861971.1:n.*478dup
NR_156186.1:n.2825dup
XM_017028810.1:c.*538dup	XP_016884299.1:n.*538dup
NM_000268.4:c.*478dup MANE Select	NP_000259.1:n.*478dup
NM_181828.3:c.*538dup	NP_861966.1:n.*538dup
NM_181829.3:c.*538dup	NP_861967.1:n.*538dup
NM_181830.3:c.*538dup	NP_861968.1:n.*538dup
NM_181832.3:c.*553dup	NP_861970.1:n.*553dup
NR_156186.2:n.2748dup
NM_181833.3:c.*478dup	NP_861971.1:n.*478dup